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rs200019422

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200019422(A;A)
Make rs200019422(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position49447669
GeneMUT
is asnp
is mentioned by
dbSNPrs200019422
ebirs200019422
HLIrs200019422
Exacrs200019422
Varsomers200019422
Maprs200019422
PheGenIrs200019422
hapmaprs200019422
1000 genomesrs200019422
hgdprs200019422
ensemblrs200019422
gopubmedrs200019422
geneviewrs200019422
scholarrs200019422
googlers200019422
pharmgkbrs200019422
gwascentralrs200019422
openSNPrs200019422
23andMers200019422
23andMe allrs200019422
SNP Nexus

SNPshotrs200019422
SNPdbers200019422
MSV3drs200019422
GWAS Ctlgrs200019422
Max Magnitude0
ClinVar
Risk rs200019422(A;A)
Alt rs200019422(A;A)
Reference rs200019422(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MUT
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.49415382C>A
CLNSRC
CLNACC RCV000186049.1,